Best practices for variant calling in clinical seq：Best practices for variant calling in clinical sequencing
Best practices for variant calling in clinical sequencing
由DCKoboldt著作·2020·被引用316次—Variantallelesshouldbesupportedbyreadsonbothstrandswithnoapparentbiasinreadposition,basequality,ormappingquality.High- ...。其他文章還包含有：「Bestpracticesforvariantcallinginclinicalsequencing」、「Bestpracticesfortheinterpretationandreportingofclinical...」、「(PDF)Bestpracticesforvariantcallinginclinicalsequencing」、「Bestpracticesforvariantcallinginclinic...
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Best practices for variant calling in clinical sequencing
https://www.ncbi.nlm.nih.gov
Variant alleles should be supported by reads on both strands with no apparent bias in read position, base quality, or mapping quality. High- ...
Best practices for the interpretation and reporting of clinical ...
https://www.nature.com
Secondary analysis involves bioinformatic processes such as alignment of the raw sequence data to a genome reference, variant calling, and ...
(PDF) Best practices for variant calling in clinical sequencing
https://www.researchgate.net
The quality of NGS calls varies widely and is influenced by features like reference sequence characteristics, read depth, and mapping accuracy.
Best practices for variant calling in clinical sequencing.
http://search.ebscohost.com
Title: Best practices for variant calling in clinical sequencing. ; Language: English ; Authors: Koboldt, Daniel C. · (AUTHOR) Daniel.Koboldt@nationwidechildrens.